ArticleESC heart failure2023
Heart failure risk scores in advanced heart failure patients: insights from the LEVO-D registry.
Article in ESC heart failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 8 citations in OpenAlex.
- Simultaneous vaccination against influenza and respiratory syncytial virus in high-risk heart failure patients.ESC heart failure · 2025Trial
- Low-dose levosimendan infusions in advanced heart failure: efficacy, safety, and factors associated with outcomes.Clinical research in cardiology : official journal of the German Cardiac Society · 2026Article
- Plasma proteomics improves risk prediction in heart failure and reveals unique biology in chronic chagas cardiomyopathy.PLoS neglected tropical diseases · 2026Article
- PIFA-N Multifactor Model to Predict Adverse Outcomes for Chronic Heart Failure Patients.Journal of clinical medicine research · 2026Article
- Performance of the MAGGIC Score in Individuals with Heart Failure: Validation in a Brazilian Population.Arquivos brasileiros de cardiologia · 2026Article
- Predicting survival in patients with severe heart failure: Risk score validation in the HELP-HF cohort.European journal of heart failure · 2025Observational
- Heart failure risk scores in advanced heart failure patients: insights from the LEVO-D registry.ESC heart failure · 2023Article
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Authors and funding
8 authors at 5 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
aimsThe prevalence of advanced heart failure (HF) is increasing due to the growing number of patients with HF and their better treatment and survival. There is a scarcity of data on the accuracy of HF web-based risk scores in this selected population. This study aimed to assess mortality prediction performance of the Meta-Analysis Global Group in Chronic HF (MAGGIC-HF) risk score and the model of the Barcelona Bio-HF Risk Calculator (BCN-Bio-HF) containing N terminal pro brain natriuretic peptide in HF patients receiving intermittent inotropic support with levosimendan as destination therapy. METHODS AND
resultsFour hundred and three advanced HF patients from 23 tertiary hospitals in Spain receiving intermittent inotropic support with levosimendan as destination therapy were included. Discrimination for all-cause mortality was compared by area under the curve (AUC) and Harrell's C-statistic at 1 year. Calibration was assessed by calibration plots comparing observed versus expected events based on estimated risk by each calculator. The included patients were predominantly men, aged 71.5 [interquartile range 64-78] years, with reduced left ventricular ejection fraction (27.5 ± 9.4%); ischaemic heart disease was the most prevalent aetiology (52.5%). Death rate at 1 year was 26.8%, while the predicted 1-year mortality by BCN-Bio-HF and MAGGIC-HF was 17.0% and 22.1%, respectively. BCN-Bio-HF AUC was 0.66 (Harrell's C-statistic 0.64), and MAGGIC-HF AUC was 0.62 (Harrell's C-statistic 0.61).
conclusionsThe two evaluated risk scores showed suboptimal discrimination and calibration with an underestimation of risk in advanced HF patients receiving levosimendan as destination therapy. There is a need for specific scores for advanced HF.
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